US3906027A - N-(perfluoroalkyl-sulphonyl)-carbamic acid esters of polyalkylene oxides - Google Patents

N-(perfluoroalkyl-sulphonyl)-carbamic acid esters of polyalkylene oxides Download PDF

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US3906027A
US3906027A US381313A US38131373A US3906027A US 3906027 A US3906027 A US 3906027A US 381313 A US381313 A US 381313A US 38131373 A US38131373 A US 38131373A US 3906027 A US3906027 A US 3906027A
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perfluoroalkyl
carbon atoms
sulphonyl
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carbamic acid
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Johann Nikolaus Meussdoerffer
Hans Niederprum
Manfred Dahm
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Bayer AG
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    • C—CHEMISTRY; METALLURGY
    • C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
    • C08J—WORKING-UP; GENERAL PROCESSES OF COMPOUNDING; AFTER-TREATMENT NOT COVERED BY SUBCLASSES C08B, C08C, C08F, C08G or C08H
    • C08J9/00—Working-up of macromolecular substances to porous or cellular articles or materials; After-treatment thereof
    • C08J9/0061—Working-up of macromolecular substances to porous or cellular articles or materials; After-treatment thereof characterized by the use of several polymeric components
    • C—CHEMISTRY; METALLURGY
    • C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
    • C08G—MACROMOLECULAR COMPOUNDS OBTAINED OTHERWISE THAN BY REACTIONS ONLY INVOLVING UNSATURATED CARBON-TO-CARBON BONDS
    • C08G65/00—Macromolecular compounds obtained by reactions forming an ether link in the main chain of the macromolecule
    • C08G65/02—Macromolecular compounds obtained by reactions forming an ether link in the main chain of the macromolecule from cyclic ethers by opening of the heterocyclic ring
    • C08G65/32—Polymers modified by chemical after-treatment
    • C08G65/329—Polymers modified by chemical after-treatment with organic compounds
    • C08G65/334—Polymers modified by chemical after-treatment with organic compounds containing sulfur
    • C08G65/3348—Polymers modified by chemical after-treatment with organic compounds containing sulfur containing nitrogen in addition to sulfur
    • C—CHEMISTRY; METALLURGY
    • C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
    • C08J—WORKING-UP; GENERAL PROCESSES OF COMPOUNDING; AFTER-TREATMENT NOT COVERED BY SUBCLASSES C08B, C08C, C08F, C08G or C08H
    • C08J2471/00—Characterised by the use of polyethers obtained by reactions forming an ether link in the main chain; Derivatives of such polymers

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  • ABSTRACT An N-(perfluoroalkyl-sulphonyl)-carbamic acid ester of a polyalkylene oxide of the formula:
  • R is a perfluoroalkyl radical of up to 20 carbon atoms, R is hydrogen, alkyl, hydroxyalkyl, cycloalkyl,
  • R is a polyoxyalkylene radical, and R is alkyl of up to 8 carbon atoms, alkenyl, aralkyl
  • the compounds are produced by reacting a perfluoroalkylsulphonamide with a chloroformic acid ester of a polyalkylene oxide in the presence of an acid binding agent.
  • the products are useful as surfactants in making polyurethane foams.
  • R represents a perfluoroalkyl group having 4 to 12 carbon atoms;
  • R is either hydrogen, a lower alkyl group or R,
  • R is a polyalkoxy group of the following structure:
  • R" represents hydrogen or methyl
  • m is the number 2 or 3
  • n a number in the range of from 2 to 20.
  • IPolyethers containing perfluoroalkyl groups cannot be directly produced from the correspondingly substituted perfluoroalkyl sulphonamides with cyclic carbonates or sulphites jb ecause hydroxy alkylation stops at the primary addition product stage (cf. German Offenlegungsschrift No. 2,024,909).
  • the object of this invention is to obtain new, non-ionogenic polyethers containing perfluoroalkyl groups through a simple reaction carried out with readily available, inexpensive starting materials.
  • the present invention relates to an N- (perfluoroalkylsulphonyl)-carbamic acid ester of a polyalkylene oxide of the formula:
  • R is a perfluoroalkyl radical of up to 20 carbon atoms
  • R is hydrogen, alkyl, hydroxyalkyl, cycloalkyl, alkenyl, aralkyl, or
  • R is a polyoxyalkylene radical, and R is alkyl of up to 8 carbon atoms, alkenyl, aralkyl
  • the carbon chain of R may be linear, branched or cyclic and preferably is of up to about 8 carbon atoms, e.g. about 4 to 8 carbon atoms.
  • R is preferably hydrogen, alkyl of up to about 18 carbon atoms, hydroxylower alkyl of up to about 4 carbon atoms, cycloalkyl of 5 or 6 carbon atoms, lower alkenyl of up to about 4 carbon atoms, phenyl-substituted lower alkyl of up to about 4 carbon atoms or lower alkoxy-lower alkyl of up to about 4 carbon atoms in each alkyl radical.
  • R is preferably made up of the structural units (CH- -CH O),, and (CH CHCH O),, wherein m and n are from 0 to about 200 but are not both simultaneously O; advantageously the sum of m and n is about 2 to 25.
  • perfluoroalkane sulphonamides used as starting materials can readily be obtained by reacting ammonia or primary amines with perfluoroalkane sulphonyl fluorides which can be obtained relatively easily by electrochemical fluorination.
  • the chloroformic acid esters of the hydroxyfunctional polyethers can be synthesized from phosgene and alcohol in accordance with the methods gencrally used for producing chlorocarbonic acid esters.
  • Tertiary amines are generally used as the proton acceptors.
  • suitable proton acceptors are trialkylamines such as triethylamine or tripropylamine, pyridine or picoline.
  • reaction is carried out at temperatures in the range of about l0 to 150C, preferably at the boiling point of the solvent used. Subsequent separation of the deposit precipitated and working up of the reaction mixture are carried out in the usual way.
  • Reaction of the perfluoroalkyl sulphonamides with the chloroformic acid esters is carried out in inert solvents, for example toluene, benzene or xylene, in the presence of proton acceptors, for example in accordance with the following equations:
  • EXAMPLE 1 250 g of the chloroformic acid ester of an w-monohydroxy-functional polyether containing ethylene oxide and propylene oxide units in a statistical ratio of l l, end-capped with butanol, having a molecular weight of approximately 1500 and a hydrolyzable chlorine content of 2.2%, were dissolved with 77.4 g of perfluoroctane sulphonamide in 200 ml of anhydrous toluene at a temperature of approximately 60C, followed by the addition of 22 ml of triethylamine. Triethyl ammonium hydrochloride was immediately precipitated in an exothermic reaction.
  • EXAMPLE 2 250 g of the chloroformic acid ester of an w-monohydroxy-functional block polyether (ethylene oxide and propylene oxide units in a ratio of l l, end-capped with butanol, having a molecular weight of approximately 1500 and a hydrolyzable chlorine content of 2.4%) were dissolved with 58 g of N-(B-hydroxyethybperfluorobutane sulphonamide in 250 ml of toluene, followed by the addition of 18 g of triethylamine.
  • w-monohydroxy-functional block polyether ethylene oxide and propylene oxide units in a ratio of l l, end-capped with butanol, having a molecular weight of approximately 1500 and a hydrolyzable chlorine content of 2.46%
  • EXAMPLE 3 122 g of the chloroformic acid ester of an w-monohydroxy-functional pure polyethylene oxide ether, also capped with butanol, having a molecular weight of 570 and a hydrolyzable chlorine content of 6.1%, were reacted with 108 g of N-methyl perfluorooctane sulphonamide in 200 ml of toluene and 22 g of triethylamine. The reaction mixture was kept for 20 minutes at 80C and then worked up in the same way as in Example 1.
  • EXAMPLE 4 200 g of the same chloroformic acid ester as in Example l (hydrolyzable chlorine content 2.2%) were reacted with 63 g of N-methyl perfluorooctane sulphonamide and 18 ml of triethylamine in 250 ml of dry toluene at a temperature of 80C. The reaction was over after minutes and the reaction product could be worked up in the same way as described in detail in Example l.
  • the pale yellow oil had a viscosity ":7 of 340 cP and a refractive index n of 2.4423.
  • This oil solidified into a wax-like mass after prolonged standing (approximately 1 week).
  • EXAMPLE 5 148 g of the chloroformic acid ester of an w-monohydroxy-functional polyether with a statistical distribution of ethylene oxide and propylene oxide .units of l 1 in the chain, having an average molecular weight of 578 and a hydrolyzable chlorine content of 5.7%, were reacted with 122 g of N-methyl perfluorooctane sulphonamide and 24 g of triethylamine in 200 ml of absolute toluene at a temperature'of C.
  • the precipitation of triethylammonium hydrochloride was over after 30 minutes and the salt could be isolated in a yield of 98%.
  • Working up was carried out in the same way as described in detail in Example 1.
  • the pale yellow oil had a refractive index m, of 1.4153 and a viscosity 1; of 130 cP.
  • EXAMPLE 6 This Example demonstrates the effectiveness of the compounds according to the invention as surfactants in various substrates.
  • the depression in surface tension is a measure of the surfactant activity.
  • polyester polyester
  • polyester 17 of product of Example 3 33.8
  • polyester with a hydroxyl number of 60 and an average molecular weight of 2500 obtained y condensing 1.0 mole of adipic acid with 1.24 moles of diethylene glycol and 0.085 mole of trimethylol propane.
  • polyethcr based on glycerol which contains ethylene oxide and propylene oxide units and 637: of terminal primary hydroxyl groups, hydroxyl number 32, average molecular weight 5200.
  • EXAMPLE 7 This Example demonstrates the effectiveness of the compounds as stabilizers in the production of polyurethane foams.
  • a weakly branched polyester obtained by condensing 1.0 mole of adipic acid, 1.24 mole of diethylene glycol and 0.085 mole of trimethylol propane (molecular weight 2500, hydroxyl number 60), were reacted with 3.0 parts by weight of water.
  • the foam had a fine pore structure. When the test was repeated without the compound of Example 1, the foam collapsed.
  • EXAMPLE 8 The test of Example 7 was repeated except that 1.0 part by weight of the compound of Example 2 according to the invention was used as foam stabilizer. Once again, a fine-pored polyester-based polyurethane foam was formed. Without the compound of Example 2, the foam collapsed.
  • R is perfluoroalkyl of up to 20 carbon atoms
  • R is hydrogen or alkyl of up to about 18 carbon atoms, hydroxy-alkyl of up to about 4 carbon atoms, cycloalkyl of 5 or 6 carbon atoms, alkenyl of up to about 4 carbon atoms, phenyl-substituted alkyl of up to about 4 carbon atoms or alkoxylower alkyl of up to about 4 carbon atoms in each alkyl radical, or
  • esters as claimed in claim 1 in which:
  • R is perfluoroalkyl of about 4 to 8 carbon atoms
  • R is lower alkyl

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  • Chemical & Material Sciences (AREA)
  • Organic Chemistry (AREA)
  • Health & Medical Sciences (AREA)
  • Chemical Kinetics & Catalysis (AREA)
  • Medicinal Chemistry (AREA)
  • Polymers & Plastics (AREA)
  • General Chemical & Material Sciences (AREA)
  • Engineering & Computer Science (AREA)
  • Materials Engineering (AREA)
  • Organic Low-Molecular-Weight Compounds And Preparation Thereof (AREA)
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Abstract

An N-(perfluoroalkyl-sulphonyl)-carbamic acid ester of a polyalkylene oxide of the formula:

in which: RF is a perfluoroalkyl radical of up to 20 carbon atoms, R1 is hydrogen, alkyl, hydroxyalkyl, cycloalkyl, alkenyl, aralkyl, or

R2 is a polyoxyalkylene radical, and R3 is alkyl of up to 8 carbon atoms, alkenyl, aralkyl or

The compounds are produced by reacting a perfluoroalkylsulphonamide with a chloroformic acid ester of a polyalkylene oxide in the presence of an acid binding agent. The products are useful as surfactants in making polyurethane foams.

Description

Uite States atet [19] Meussdoerffer et a1.
[4 1 Sept. 16, 1975 54 1 N-( PERFLUOROALKYL-SULPHONYL CARBAMIC ACID ESTERS OF POLYALKYLENE OXIDES [75] Inventors: Johann Nikolaus Meussdoerffer,
Blecher; Hans Niederpriim, Monheim, Rhineland; Manfred Dahm, Bergisch-Neukirchen, all of Germany [73] Assignee: Bayer Aktiengesellschaft,
Leverkusen, Germany [22] Filed: July 20, 1973 [21] App1.No.: 381,313
3,357,932 12/1967 Heydkamp et a1.
3,562,290 2/1971 Fawzi 260/481 C 3,663,708 5/1972 Harrington 260/470 3,725,451 4/1973 Trancik 260/470 3,799,968 3/1974 Harrington et a1. 260/470 3,840,527 10/1974 Moore ct a1. 260/470 OTHER PUBLICATIONS March, Advanced Organic Chemistry,
McGraw-Hill, N.Y., (1908), p. 335,
Primary ExaminerJohn F. Terapane Attorney, Agent, or FirmBurgess, Dinklage & Sprung [5 7] ABSTRACT An N-(perfluoroalkyl-sulphonyl)-carbamic acid ester of a polyalkylene oxide of the formula:
in which:
R is a perfluoroalkyl radical of up to 20 carbon atoms, R is hydrogen, alkyl, hydroxyalkyl, cycloalkyl,
alkenyl', aralkyl, or
R is a polyoxyalkylene radical, and R is alkyl of up to 8 carbon atoms, alkenyl, aralkyl The compounds are produced by reacting a perfluoroalkylsulphonamide with a chloroformic acid ester of a polyalkylene oxide in the presence of an acid binding agent. The products are useful as surfactants in making polyurethane foams.
3 Claims, No Drawings I N.-(PERFLUOROALKYL-SULPHONYL)- CARBAMIC ACID ESTERS OF POLYALKYLENE OXIDES The present I invention relates to N- (perfluoroalkylsulfonyl)-carbamic acid esters of polyalkyle'ne oxides and to a process for their production in which primary or secondary perfluoroalkyl sulphoamides are reacted with chloroformicacid esters of the corresponding hydroxyfunctional polyethers in the presence of proton acceptors.
in which:
R, represents a perfluoroalkyl group having 4 to 12 carbon atoms; R is either hydrogen, a lower alkyl group or R, R is a polyalkoxy group of the following structure:
in which:
R" represents hydrogen or methyl, m is the number 2 or 3 and n a number in the range of from 2 to 20. Unfortunately, the methods for producing these compounds by condensing ethylene or propylene oxide with correspondingly substituted perfluoroalkyl sulphonamido alkanols in alkali medium or by condensing the sodium salt of a perfluoroalkyl sulphonamide with a polyethylene glycol halide, are attended by considerable disadvantages.
Apart from the unavailability of some of the polyethers used, the extremely long reaction times of up to 16 hours represent a particularly serious disadvantage because decomposition of the. sensitive polyether groups can occuir at the necessary temperatures. Furthermore, some reactions have to be carried out under pressure with the result that elaborate apparatus have to be used for large-scale working. At the same time, however, compounds with an extremely variable polyether chain structure are also formed. Unfortunately, subsequent purification is not possible.
IPolyethers containing perfluoroalkyl groups cannot be directly produced from the correspondingly substituted perfluoroalkyl sulphonamides with cyclic carbonates or sulphites jb ecause hydroxy alkylation stops at the primary addition product stage (cf. German Offenlegungsschrift No. 2,024,909).
Accordingly, the object of this invention is to obtain new, non-ionogenic polyethers containing perfluoroalkyl groups through a simple reaction carried out with readily available, inexpensive starting materials.
The present invention relates to an N- (perfluoroalkylsulphonyl)-carbamic acid ester of a polyalkylene oxide of the formula:
in which:
R is a perfluoroalkyl radical of up to 20 carbon atoms,
R is hydrogen, alkyl, hydroxyalkyl, cycloalkyl, alkenyl, aralkyl, or
R is a polyoxyalkylene radical, and R is alkyl of up to 8 carbon atoms, alkenyl, aralkyl The carbon chain of R may be linear, branched or cyclic and preferably is of up to about 8 carbon atoms, e.g. about 4 to 8 carbon atoms. R is preferably hydrogen, alkyl of up to about 18 carbon atoms, hydroxylower alkyl of up to about 4 carbon atoms, cycloalkyl of 5 or 6 carbon atoms, lower alkenyl of up to about 4 carbon atoms, phenyl-substituted lower alkyl of up to about 4 carbon atoms or lower alkoxy-lower alkyl of up to about 4 carbon atoms in each alkyl radical. R is preferably made up of the structural units (CH- -CH O),, and (CH CHCH O),,, wherein m and n are from 0 to about 200 but are not both simultaneously O; advantageously the sum of m and n is about 2 to 25.
Among these polyethers, those compounds still containing free OH groups are particularly valuable. In the most simple case, R is thus hydroxyethyl, CH CH- 0H, so that they will undergo reactions with isocyanates and, hence, can be directly incorporated into plastic systems. The hydroxyalkyl-functional perfluoroalkane sulphonamides required for this purpose can be readily obtained in quantitative yields through the reaction of primary perfluoroalkane sulphonamides with cyclic carbonates or sulphites (cf. German Offenlegungsschrift No. 2,024,909).
The perfluoroalkane sulphonamides used as starting materials can readily be obtained by reacting ammonia or primary amines with perfluoroalkane sulphonyl fluorides which can be obtained relatively easily by electrochemical fluorination.
The following are examples of the perfluoroalkyl sulphonamides to be used:
The chloroformic acid esters of the hydroxyfunctional polyethers can be synthesized from phosgene and alcohol in accordance with the methods gencrally used for producing chlorocarbonic acid esters.
Tertiary amines are generally used as the proton acceptors. Examples of suitable proton acceptors are trialkylamines such as triethylamine or tripropylamine, pyridine or picoline.
The reaction is carried out at temperatures in the range of about l0 to 150C, preferably at the boiling point of the solvent used. Subsequent separation of the deposit precipitated and working up of the reaction mixture are carried out in the usual way.
Among the large number of possible substances according to the invention, the following are mentioned by way of example:
average molecular hours, after which the solvent can be distilled off and most of the excess phosgene and hydrogen chloride formed escapes. Residues of phosgene, hydrogen chloride and solvent are removed by heating in vacuo at a temperature of about 100C. The hydrolyzable chlorine content of the reaction product is analytically determined by reaction with dibutylamine and back titration with hydrochloric acid.
Reaction of the perfluoroalkyl sulphonamides with the chloroformic acid esters is carried out in inert solvents, for example toluene, benzene or xylene, in the presence of proton acceptors, for example in accordance with the following equations:
( 0 Examples. The products obtained in accordance with the invention were identified with the aid of nuclearresonance spectra, lR-spectra and by elementalanalyses.
EXAMPLE 1 250 g of the chloroformic acid ester of an w-monohydroxy-functional polyether containing ethylene oxide and propylene oxide units in a statistical ratio of l l, end-capped with butanol, having a molecular weight of approximately 1500 and a hydrolyzable chlorine content of 2.2%, were dissolved with 77.4 g of perfluoroctane sulphonamide in 200 ml of anhydrous toluene at a temperature of approximately 60C, followed by the addition of 22 ml of triethylamine. Triethyl ammonium hydrochloride was immediately precipitated in an exothermic reaction. The reaction temperature was then maintained at about 80C for 30 minutes, after which the salt precipitated was filtered off and the clear filtrate freed in vacuo (approximately mm Hg) from the solvent in a rotary evaporator. A pale yellow oil was left behind, after prolonged standing solidifying into a wax-like mass. 1 I
0.05% of hydrolyzable chloride could still be detected in the reaction product. 95% of the salt separated off consisted of triethyl ammonium hydrochloride.
EXAMPLE 2 250 g of the chloroformic acid ester of an w-monohydroxy-functional block polyether (ethylene oxide and propylene oxide units in a ratio of l l, end-capped with butanol, having a molecular weight of approximately 1500 and a hydrolyzable chlorine content of 2.4%) were dissolved with 58 g of N-(B-hydroxyethybperfluorobutane sulphonamide in 250 ml of toluene, followed by the addition of 18 g of triethylamine. The
separation of triethyl ammonium hydrochloride was quantitative after only 20 minutes at 80C. Working up was carried out as in Example 1. The reaction product had a molecular weight of approximately 1800. The triethyl ammonium hydrochloride was obtained in a yield of 96%. A residue of only 0.01% of hydrolyzable chlorine was detected in the reaction product.
EXAMPLE 3 122 g of the chloroformic acid ester of an w-monohydroxy-functional pure polyethylene oxide ether, also capped with butanol, having a molecular weight of 570 and a hydrolyzable chlorine content of 6.1%, were reacted with 108 g of N-methyl perfluorooctane sulphonamide in 200 ml of toluene and 22 g of triethylamine. The reaction mixture was kept for 20 minutes at 80C and then worked up in the same way as in Example 1.
EXAMPLE 4 200 g of the same chloroformic acid ester as in Example l (hydrolyzable chlorine content 2.2%) were reacted with 63 g of N-methyl perfluorooctane sulphonamide and 18 ml of triethylamine in 250 ml of dry toluene at a temperature of 80C. The reaction was over after minutes and the reaction product could be worked up in the same way as described in detail in Example l.
The pale yellow oil had a viscosity ":7 of 340 cP and a refractive index n of 2.4423.
This oil solidified into a wax-like mass after prolonged standing (approximately 1 week).
EXAMPLE 5 148 g of the chloroformic acid ester of an w-monohydroxy-functional polyether with a statistical distribution of ethylene oxide and propylene oxide .units of l 1 in the chain, having an average molecular weight of 578 and a hydrolyzable chlorine content of 5.7%, were reacted with 122 g of N-methyl perfluorooctane sulphonamide and 24 g of triethylamine in 200 ml of absolute toluene at a temperature'of C.
The precipitation of triethylammonium hydrochloride was over after 30 minutes and the salt could be isolated in a yield of 98%. Working up was carried out in the same way as described in detail in Example 1. The pale yellow oil had a refractive index m, of 1.4153 and a viscosity 1; of 130 cP.
EXAMPLE 6 This Example demonstrates the effectiveness of the compounds according to the invention as surfactants in various substrates. The depression in surface tension is a measure of the surfactant activity.
Substrate Surface tension (Dyn/an) I water 72.0 water 1% of product of Example 1 28.2
water 1% of product of Example 2 31.0
water 171 of product of Example 3 24.4
water 1% of product of Example 4 27.6
Polyester" 58.0
polyester" 1'71 of product of Example 1 38.2
polyester" polyester" 171 of product of Example 2 50.0
polyester 17: of product of Example 3 33.8
polyester 1% of product of Example 4 38.0
polyether" 39.0
polyether" 17! of product of Example 1 35.1
polyether" 1% of product of Example 3 36.2
"=polyester with a hydroxyl number of 60 and an average molecular weight of 2500 obtained y condensing 1.0 mole of adipic acid with 1.24 moles of diethylene glycol and 0.085 mole of trimethylol propane.
"=polyethcr based on glycerol which contains ethylene oxide and propylene oxide units and 637: of terminal primary hydroxyl groups, hydroxyl number 32, average molecular weight 5200.
EXAMPLE 7 This Example demonstrates the effectiveness of the compounds as stabilizers in the production of polyurethane foams.
parts by weight of a weakly branched polyester, obtained by condensing 1.0 mole of adipic acid, 1.24 mole of diethylene glycol and 0.085 mole of trimethylol propane (molecular weight 2500, hydroxyl number 60), were reacted with 3.0 parts by weight of water. 1.25 parts by weight of dimethyl benzylamine, 0.5 parts by weight of the compound of Example 1 according to the invention and 40 parts by weight of tolylene diisocyanate (65% of 2,4- and 35% of 2,6-isomer), to form a soft polyester-based polyurethane foam. The foam had a fine pore structure. When the test was repeated without the compound of Example 1, the foam collapsed.
EXAMPLE 8 The test of Example 7 was repeated except that 1.0 part by weight of the compound of Example 2 according to the invention was used as foam stabilizer. Once again, a fine-pored polyester-based polyurethane foam was formed. Without the compound of Example 2, the foam collapsed.
It will be appreciated that the instant specification and examples are set forth by way of illustration and not limitation, and that various modifications and changes may be made without departing from the spirit and scope of the present invention.
What is claimed is: I
l. N(Perfluoroalkylsulphonyl)-carbamic acid esters of polyalkylene glycols of the formula in which:
R is perfluoroalkyl of up to 20 carbon atoms,
R is hydrogen or alkyl of up to about 18 carbon atoms, hydroxy-alkyl of up to about 4 carbon atoms, cycloalkyl of 5 or 6 carbon atoms, alkenyl of up to about 4 carbon atoms, phenyl-substituted alkyl of up to about 4 carbon atoms or alkoxylower alkyl of up to about 4 carbon atoms in each alkyl radical, or
2. Esters as claimed in claim 1, in which:
R is perfluoroalkyl of about 4 to 8 carbon atoms,
and
R is lower alkyl.
3. Esters as claimed in claim 2, wherein the sum of m and n is about 2 to 25.

Claims (3)

1. N-(PERFLUOROALKYL-SULPHONYL)-CARBOMIC ACID ESTERS OF POLYALKYLENE GLYCOLS OF THE FORMULA
2. Esters as claimed in claim 1, in which: RF is perfluoroalkyl of about 4 to 8 carbon atoms, and R3 is lower alkyl.
3. Esters as claimed in claim 2, wherein the sum of m and n is about 2 to 25.
US381313A 1972-08-05 1973-07-20 N-(perfluoroalkyl-sulphonyl)-carbamic acid esters of polyalkylene oxides Expired - Lifetime US3906027A (en)

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US4474807A (en) * 1982-05-06 1984-10-02 Henkel Kommandigesellschaft Auf Aktien 2-(3-Iodo-2-propynyloxy)-ethyl carbamates, the preparation thereof, and their use as antimicrobial agents
US5539024A (en) * 1994-05-26 1996-07-23 Bayer Aktiengesellschaft Resins containing perfluoroalkyl groups and their use
US20060148671A1 (en) * 2004-12-30 2006-07-06 Dams Rudolf J Compositions of monomeric surfactants
US20060147645A1 (en) * 2004-12-30 2006-07-06 Dams Rudolf J Compositions containing C4-swallow tail silanes
US20060149012A1 (en) * 2004-12-30 2006-07-06 Terrazas Michael S Fluorochemical polymeric surfactants
US7164041B1 (en) 2005-11-17 2007-01-16 3M Innovative Properties Company Fluorinated Gemini surfactants
US20070049646A1 (en) * 2005-08-30 2007-03-01 Moore George G I Compositions of fluorochemical surfactants
US20080008891A1 (en) * 2006-07-05 2008-01-10 Dams Rudolf J Compositions containing silanes
US20080113882A1 (en) * 2006-02-21 2008-05-15 3M Innovative Properties Company Sandstone having a modified wettability and a method for modifying the surface energy of sandstone
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CN102351755A (en) * 2011-08-15 2012-02-15 华中师范大学 Fluorine-containing imine cationic surfactant preparation method and application thereof
WO2013155362A1 (en) 2012-04-13 2013-10-17 3M Innovative Properties Company Pressure sensitive adhesive foams and articles therefrom
US20210039060A1 (en) * 2017-04-04 2021-02-11 Harcros Chemicals, Inc. Surfactants having non-conventional hydrophobes

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GB2010874B (en) * 1977-12-07 1982-10-06 Ciba Geigy Ag Fluorinated nonionic surfactants
DE3131683A1 (en) * 1981-08-11 1983-02-24 Hoechst Ag, 6000 Frankfurt "ALKYL-SULFONAMIDO-ALKYLCARBONIC ACID ESTER, METHOD FOR THE PRODUCTION AND USE THEREOF"
DE4240008A1 (en) * 1992-11-27 1994-06-01 Bayer Ag Polyether-substituted imide compounds and their use
US5587513A (en) * 1992-11-27 1996-12-24 Pohmer; Klaus Polyether-substituted imide compounds and their use

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US4474807A (en) * 1982-05-06 1984-10-02 Henkel Kommandigesellschaft Auf Aktien 2-(3-Iodo-2-propynyloxy)-ethyl carbamates, the preparation thereof, and their use as antimicrobial agents
US5539024A (en) * 1994-05-26 1996-07-23 Bayer Aktiengesellschaft Resins containing perfluoroalkyl groups and their use
US7495118B2 (en) 2004-12-30 2009-02-24 3M Innovative Properties Company Compositions containing C4-swallow tail silanes
US20060148671A1 (en) * 2004-12-30 2006-07-06 Dams Rudolf J Compositions of monomeric surfactants
US20060149012A1 (en) * 2004-12-30 2006-07-06 Terrazas Michael S Fluorochemical polymeric surfactants
US7160850B2 (en) 2004-12-30 2007-01-09 3M Innovative Properties Company Compositions of monomeric surfactants
US7776983B2 (en) 2004-12-30 2010-08-17 3M Innovative Properties Company Fluorochemical polymeric surfactants
US20060147645A1 (en) * 2004-12-30 2006-07-06 Dams Rudolf J Compositions containing C4-swallow tail silanes
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US8536241B2 (en) 2010-06-30 2013-09-17 3M Innovative Properties Company (Meth)acryloyl pressure-sensitive foam adhesives
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WO2013155362A1 (en) 2012-04-13 2013-10-17 3M Innovative Properties Company Pressure sensitive adhesive foams and articles therefrom
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Also Published As

Publication number Publication date
DE2238740B2 (en) 1980-07-24
JPS4955623A (en) 1974-05-30
GB1418095A (en) 1975-12-17
DE2238740A1 (en) 1974-02-07
DE2238740C3 (en) 1981-07-16
IT990128B (en) 1975-06-20
NL7310787A (en) 1974-02-07
FR2194739A1 (en) 1974-03-01
FR2194739B1 (en) 1979-06-22

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